Regulatory Affairs Manager

Posted Yesterday
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Hiring Remotely in 29203, Columbia, SC, USA
In-Office or Remote
96K-125K Annually
Senior level
Pharmaceutical • Manufacturing
The Role
Lead regulatory strategy and execution for ANDA and customer-led global submissions, manage FDA submissions and responses, draft labeling, oversee lifecycle activities and adverse event reporting, mentor RA associates, monitor regulations, and support due diligence and partnerships.
Summary Generated by Built In

The Regulatory Affairs Manager is responsible for supporting development and execution of regulatory strategies for ANDA submissions as well as CDMO support for customer-led submissions (FDA and global). The Regulatory Affairs Manager will ensure compliance with regulatory requirements and manage lifecycle activities in alignment with the Director of Regulatory Affairs.


Responsibilities:

  • Provide critical support in writing and editing technical documents to support submissions for internal ANDA projects as well as customer-led global submissions.
  • Serve as primary RA contact on project teams to support product development.
  • Format, publish, and submit documentation to the FDA for initial and lifecycle submissions.
  • Respond to FDA queries and deficiencies.
  • Provide guidance to RA Associates and aid in development of team.
  • Develop and implement regulatory strategies for product development, registration, and maintenance across assigned markets.
  • Monitor and interpret new and evolving regulations and assess impact on company products.
  • Draft, review, and finalize product labeling for ANDA submissions, including structured product labeling.
  • Oversee adverse event reporting process and ensure compliance with reporting requirements.
  • Support due diligence activities, licensing, and partnerships.
Qualifications
  • Bachelor of Science in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or related field
  • 5+ years regulatory affairs experience; FDA submission experience required, experience with device and/or drug/device combination products preferred
  • Highly detail-oriented and possess considerable problem-solving and organization skills
  • Ability to work on complex projects and take initiative with general direction and minimal guidance
  • Ability to be flexible with a change in priorities
  • Excellent written, verbal, and listening skills, must work well with others
  • Experience using an electronic document control system
  • Experience with eCTD publishing software preferred
  • Proficient with Microsoft Word, Excel, PowerPoint, and Adobe Acrobat

Skills Required

  • Bachelor of Science in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or related field
  • 5+ years regulatory affairs experience
  • FDA submission experience
  • Experience with device and/or drug/device combination products
  • Experience using an electronic document control system
  • Experience with eCTD publishing software
  • Proficient with Microsoft Word, Excel, PowerPoint, and Adobe Acrobat
  • Highly detail-oriented with strong problem-solving and organization skills
  • Ability to work on complex projects independently and take initiative with minimal guidance
  • Excellent written, verbal, and listening skills and ability to work well with others
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The Company
HQ: Columbia, SC
600 Employees
Year Founded: 1995

What We Do

The Ritedose Corporation is a leading pharmaceutical contract development and manufacturing organization (CDMO) specializing in sterile Blow-Fill-Seal (BFS) technology for branded and generic medications.

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